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Role of αβ T Cell Depletion in Prevention of Graft versus Host Disease
Graft versus host disease (GVHD) represents a major complication of allogeneic hematopoietic stem cell transplantation (allo HCT). Graft cellular manipulation has been used to mitigate the risk of GVHD. The αβ T cells are considered the primary culprit for causing GVHD therefore depletion of this T...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5618293/ https://www.ncbi.nlm.nih.gov/pubmed/28672883 http://dx.doi.org/10.3390/biomedicines5030035 |
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author | Abdelhakim, Haitham Abdel-Azim, Hisham Saad, Ayman |
author_facet | Abdelhakim, Haitham Abdel-Azim, Hisham Saad, Ayman |
author_sort | Abdelhakim, Haitham |
collection | PubMed |
description | Graft versus host disease (GVHD) represents a major complication of allogeneic hematopoietic stem cell transplantation (allo HCT). Graft cellular manipulation has been used to mitigate the risk of GVHD. The αβ T cells are considered the primary culprit for causing GVHD therefore depletion of this T cell subset emerged as a promising cellular manipulation strategy to overcome the human leukocyte antigen (HLA) barrier of haploidentical (haplo) HCT. This approach is also being investigated in HLA-matched HCT. In several studies, αβ T cell depletion HCT has been performed without pharmacologic GVHD prophylaxis, thus unleashing favorable effect of donor’s natural killer cells (NK) and γδ T cells. This article will discuss the evolution of this method in clinical practice and the clinical outcome as described in different clinical trials. |
format | Online Article Text |
id | pubmed-5618293 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-56182932017-09-29 Role of αβ T Cell Depletion in Prevention of Graft versus Host Disease Abdelhakim, Haitham Abdel-Azim, Hisham Saad, Ayman Biomedicines Review Graft versus host disease (GVHD) represents a major complication of allogeneic hematopoietic stem cell transplantation (allo HCT). Graft cellular manipulation has been used to mitigate the risk of GVHD. The αβ T cells are considered the primary culprit for causing GVHD therefore depletion of this T cell subset emerged as a promising cellular manipulation strategy to overcome the human leukocyte antigen (HLA) barrier of haploidentical (haplo) HCT. This approach is also being investigated in HLA-matched HCT. In several studies, αβ T cell depletion HCT has been performed without pharmacologic GVHD prophylaxis, thus unleashing favorable effect of donor’s natural killer cells (NK) and γδ T cells. This article will discuss the evolution of this method in clinical practice and the clinical outcome as described in different clinical trials. MDPI 2017-06-26 /pmc/articles/PMC5618293/ /pubmed/28672883 http://dx.doi.org/10.3390/biomedicines5030035 Text en © 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Abdelhakim, Haitham Abdel-Azim, Hisham Saad, Ayman Role of αβ T Cell Depletion in Prevention of Graft versus Host Disease |
title | Role of αβ T Cell Depletion in Prevention of Graft versus Host Disease |
title_full | Role of αβ T Cell Depletion in Prevention of Graft versus Host Disease |
title_fullStr | Role of αβ T Cell Depletion in Prevention of Graft versus Host Disease |
title_full_unstemmed | Role of αβ T Cell Depletion in Prevention of Graft versus Host Disease |
title_short | Role of αβ T Cell Depletion in Prevention of Graft versus Host Disease |
title_sort | role of αβ t cell depletion in prevention of graft versus host disease |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5618293/ https://www.ncbi.nlm.nih.gov/pubmed/28672883 http://dx.doi.org/10.3390/biomedicines5030035 |
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